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WO2001060354A1 - Medicament anticancereux comprenant un derive d'acide anthranilique en tant qu'ingredient actif - Google Patents

Medicament anticancereux comprenant un derive d'acide anthranilique en tant qu'ingredient actif Download PDF

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Publication number
WO2001060354A1
WO2001060354A1 PCT/JP2001/001090 JP0101090W WO0160354A1 WO 2001060354 A1 WO2001060354 A1 WO 2001060354A1 JP 0101090 W JP0101090 W JP 0101090W WO 0160354 A1 WO0160354 A1 WO 0160354A1
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Prior art keywords
group
naphthalene
hydrogen atom
place
compound
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PCT/JP2001/001090
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English (en)
Japanese (ja)
Inventor
Naoki Tsuchiya
Takumi Takeyasu
Takashi Kawamura
Takao Yamori
Takashi Tsuruo
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Teijin Limited
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Priority to AU2001234089A priority Critical patent/AU2001234089B2/en
Priority to EP01906131A priority patent/EP1256341A4/fr
Priority to CA002400264A priority patent/CA2400264A1/fr
Priority to AU3408901A priority patent/AU3408901A/xx
Priority to US10/203,288 priority patent/US20030220402A1/en
Publication of WO2001060354A1 publication Critical patent/WO2001060354A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04—Five-membered rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/18—Sulfonamides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/235—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/235—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
    • A61K31/24—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group having an amino or nitro group
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/275—Nitriles; Isonitriles
    • A61K31/277—Nitriles; Isonitriles having a ring, e.g. verapamil
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • C07C235/38—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring

Definitions

  • the present invention relates to a therapeutic agent for cancer containing an anthranilic acid derivative or a pharmaceutically acceptable salt thereof as an active ingredient. More specifically, the present invention relates to a therapeutic agent for cancer comprising an anthranilic acid derivative having an anthranilic acid skeleton and a benzene skeleton and further having a benzene skeleton or a naphthylene skeleton or a pharmaceutically acceptable salt thereof as an active ingredient.
  • Background art
  • the anticancer activity based on the cytotoxic activity of a compound having an aryl skeleton is described in, for example, a substituted phenylsulfonyl derivative (Japanese Patent Application Laid-Open No. 5-91770), a 2-arylquinolinol derivative (Japanese Patent Application Laid-Open No. No. 3,743,397) and benzoyl acetylene derivatives (Japanese Patent Application Laid-Open No. 7-97350).
  • An object of the present invention is to provide a novel therapeutic agent for cancer.
  • an anthranilic acid derivative has a cytotoxic effect on highly proliferative cell types under the above-mentioned problems. It has also been found that this has a strong growth inhibitory or cytotoxic effect on human cancer cells. Therefore, a pharmaceutical composition containing these anthranilic acid derivatives, pharmaceutically acceptable salts thereof, or pharmaceutically acceptable solvates thereof as active ingredients is useful as a therapeutic agent for cancer.
  • X represents a group selected from the following formula (2) or formula (2) -2,
  • R 1 and R 2 are The respective independently, a hydrogen atom, a hydroxyl group, trihalomethyl group, one C 12 chain if Ku cyclic hydrocarbon group and Okishi group or Chio consisting alkoxy group if Ku alkylthio group, Ariru group moiety halogen atom C 7 — which may be substituted by one or more of a methyl group or a methyloxy group; C 3 — which may be substituted by an aralkyloxy group of Cii or one or more phenyl groups. Represents an alkenyloxy group.
  • R 4 and R 5 each independently represent a hydrogen atom, a halogen atom, a C 1 -C 4 alkyl group, or a Ci-C 4 -alkoxy group.
  • Y is a hydrogen atom, a halogen atom, a nitro group, a nitrile group, an amino group, —CO OR 7 , — NHCOR 8 , one NHS ⁇ 2 R 9 (where R 7 is a hydrogen atom or a C i -C 4 alkyl And R 8 and R 9 each independently represent an alkyl group of ⁇ —C 4 .
  • G is a hydrogen atom, a hydroxyl group, —SO 2 NH 2 , —COOR 3 (where R 3 represents a hydrogen atom or a C 4 alkyl group), —CN, or tetrazole— Represents a group,
  • Z represents a hydrogen atom, a halogen atom, a nitro group, or a methyl group.
  • An anthranilic acid derivative represented by the formula or a pharmaceutically acceptable salt thereof is provided as an active ingredient.
  • the present invention also provides a method for treating cancer using a drug containing the above anthranilic acid derivative or a pharmaceutically acceptable salt thereof.
  • the present invention relates to the use of the above anthranilic acid derivative or a pharmaceutically acceptable salt thereof for producing a therapeutic agent for cancer.
  • R 1 and R 2 each independently represent a hydrogen atom, a hydroxyl group, a trihalomethyl Or an alkoxy or alkylthio group consisting of a C i-Cu chain or cyclic hydrocarbon group and an oxy or thio group, wherein the aryl group is at least one of a halogen atom, a methyl group, or a methyloxy group Represents a C 7 -C i i7 laralkyloxy group which may be substituted by, or a C 3 -C 10 alkenyloxy group which may be substituted by one or more phenyl groups.
  • R 1 or R 2 represents a C 12 linear or cyclic alkyloxy group, for example, a methyloxy group, an ethyloxy group, a propyloxy group, a 2-propyloxy group, a (1-1 or 2-) methylpropyloxy group , 2, 2-dimethylpropyloxy, (n- or tert-) butyloxy, 2-ethylbutyloxy, (2- or 3-) methylbutyloxy, pentyloxy, hexyloxy Group, heptyloxy group, octyloxy group, decyloxy group, dodecyloxy group, cyclopropyloxy group, cyclopropylmethyloxy group, cyclobutyloxy group, cyclopentyloxy group, cyclohexyloxy group, cyclohexylmethyloxy group , Cyclooctyloxy, cycloheptyloxy, cyclododecyl It can be
  • R 1 or R 2 is C! -0 12, for example, a methylthio group, Echiruchio group, propylthio group, 2-pro Piruchio group, (1 one or 2) methyl Propylthio, 2,2-dimethylpropylthio, (n- or tert-) butylthio, 2-ethylbutylthio, (2- or 3-) methylbutylthio, pentylthio, hexylthio, Butylthio, octylthio, decylthio, dodecylthio, cyclopropylthio, cyclopropylmethylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, cyclohexylmethylthio, cyclooctylthio, cyclohexyl Butylthio group, cycl
  • R 1 or R 2 represents an aralkyloxy group of C 7 —C ⁇ 2
  • the aryl group of the aralkyloxy group is substituted with one or more of a halogen atom, a methyl group, or a methyloxy group.
  • substituents include a fluorine atom, a chlorine atom, a bromine atom, a methyl group and a methyloxy group.
  • the aralkyloxy group represented by R 1 may be, for example, a benzyloxy group, a (2-, 3-, or 4-) chlorobenzyl group, a (2_, 3-, or 4-) methoxybenzyl Oxy, (2-1, 3- or 4-) methylbenzyloxy, ( ⁇ - or 3-) phenethyloxy, 3-phenylphenyloxy, 2-phenyl-2-propyloxy , 2-phenyl-1-cyclohexyloxy, (1-phenylcyclopropyl) methyloxy, (1-phenylcyclopentyl) methyloxy, (1-1 or 2-) naphthylmethyloxy, etc. You can choose.
  • R 1 or R 2 is —. May be an alkenyloxy group.
  • the alkenyloxy group in this case includes, for example, aryloxy, methallyloxy, crotyloxy, 3-butenyloxy, 4-pentenyloxy, 5-hexenyloxy, 7-octenyloxy, geranyoxy, cinnamyloxy, 2 —Cyclohexenyloxy group, (3-cyclohexenyl) methyloxy group, 1,4-pentyl-1-yloxy group, etc.
  • R 1 and R 2 may be a hydrogen atom, a hydroxyl group, or a trihalomethyl group.
  • the halogen atom when representing a trihalomethyl group include a fluorine atom and a chlorine atom.
  • atoms or groups represented by R 1 or R 2 preferred are a hydrogen atom, a hydroxyl group, a methyloxy group, an ethyloxy group, a hydroxypyroxy group, a 2-propyloxy group, 2—) Methyl propyloxy group, 2,2-dimethylpropyloxy group, ( ⁇ - or tert-) butoxy group, 2-ethylbutyloxy group, (2- or 3-) Tylbutyloxy, pentyloxy, hexyloxy, heptyloxy, octyloxy, decyloxy, dodecyloxy, cyclopropylmethyloxy, cyclopentyloxy, cyclohexyloxy, cyclohexylmethyloxy, cyclooctyloxy Xy, cycloheptyloxy, cyclododecyloxy, methylthio, ethylthio, is
  • R 1 or R 2 groups are hydrogen atoms Of these, hydroxyl, C i one C 1 2 of chain or Arukiruokishi group consisting of cyclic saturated hydrocarbon or C 7, - those wherein C 1 2 of Ararukiruokishi groups Particularly preferred. More preferably, a hydrogen atom, for example, a C 5 —Ci 2 cyclic saturated alkoxy group such as a cyclohexyloxy group, a cycloheptyloxy group, a cyclooctyloxy group, a cyclopentyloxy group, a cyclododecanyloxy group, or C 3 — C 8 is a branched, saturated alkoxy group. Particularly preferred are an alkyloxy group branched from a carbon adjacent to an oxygen atom, for example, an isopropyloxy group, a 3-pentyloxy group, or a benzyloxy group.
  • R 1 and R 2 may be substituted at any position on the naphthalene down ring on to a benzene ring, but preferably R 1 is naphthyl evening Ren in which counted from ring a on the ring is bonded 6-position (a is being replaced in the 2-position) R 2 to free is located at the 4-position counted from the binding of a on the benzene ring .
  • R 4 and R 5 each independently represent a hydrogen atom, a halogen atom, a C i —C 4 alkyl group, or an (: —C 4 alkoxy group. Fluorine, chlorine, bromine, etc.
  • the C 4 alkyl group include a methyl group, an ethyl group, an isopropyl group and a t-butyl group.
  • the C i -C 4 alkoxy group include a -methyloxy group, an ethyloxy group, an isopropyloxy group, a t-butyloxy group and the like.
  • R 4 or R 5 is preferably a hydrogen atom, a chlorine atom, a methyl group, or a methyloxy group. Among them, a hydrogen atom is preferable.
  • R 4 is substituted at the 2-position on the benzene ring, and R 5 is substituted at the 3-position on the benzene ring.
  • R 6 represents a hydrogen atom or —C 4 alkyl group.
  • R 6 is preferably a hydrogen atom or a methyl group. And more preferably a bond as A; —O— or —S—.
  • Y represents a hydrogen atom, a halogen atom, a nitro group, a nitrile group, an amino group, —C ⁇ R 7 (where R 7 represents a hydrogen atom or —C 4 alkyl group). ), —NHCOR 8 , or —NHSO 2 R 9 (where R 8 and R 9 each independently represent a Ci—C 4 alkyl group).
  • R 8 and R 9 each independently represent a Ci—C 4 alkyl group.
  • examples of the halogen atom include a fluorine atom, a chlorine atom, and a bromine atom, and among them, a chlorine atom is preferable.
  • R 7 is a hydrogen atom or a C E - represents an alkyl group of C 4, for example, a hydrogen atom, a methyl group, Echiru group, n- propyl group, 2-propyl group, n-butyl group and tert-butyl group.
  • Preferred one COOR 7 is one COOH or —C ⁇ CH 3 .
  • R 8 or R 9 is (: represents an alkyl group of C 4. For example, methyl group, ethyl group, n-propyl group, 2-propyl .
  • G represents a hydrogen atom, a hydroxyl group, —SO 2 NH 2 , —COOR 3 (where R 3 represents a hydrogen atom or a C—C 4 alkyl group), one CN, Or a tetrazole-5-yl group.
  • R 3 represents a hydrogen atom or a C—C 4 alkyl group
  • G is - representative of the COOR 3, examples of the alkyl group represented by R 3, methyl, Echiru group, (n-, an iso-) propyl group, (n-, iso-, tert-) butyl group and the like No.
  • —C ⁇ R 3 (R 3 represents a hydrogen atom or an alkyl group of C ⁇ —C 4 ) or a tetrazol-5-yl group is preferable, and particularly, R 3 is a hydrogen atom, a methyl group, or Those which are ethyl groups are preferred. G is more preferably 1CO ⁇ H or a tetrazo-1-yl 5-yl group.
  • Z represents a hydrogen atom, a halogen atom, a nitro group, or a methyl group.
  • the halogen atom include a fluorine atom, a chlorine atom, and a bromine atom.
  • Z is preferably a hydrogen atom, a fluorine atom, a chlorine atom, or a methyl group, and particularly preferably a hydrogen atom.
  • Such compounds exhibit particularly high cytotoxic effects on strongly proliferating cells.
  • R 1 and R 2 each represent a hydrogen atom, a C 5 —C 12 cyclic alkyl group, a C 3 —C 8 branched alkyl group, or a benzyl group.
  • A represents a bond; one represents O—, E represents a bond— C
  • H 2 C ( ⁇ ) — and G represents —C—OH or a tetrazo-1-yl group.
  • Such compounds show even stronger cytotoxic effects.
  • this substituent when Z represents a halogen atom or a methyl group, this substituent is preferably located at the 4- or 5-position with respect to the G group of the benzene ring to which it is bonded. .
  • Such a Z group located at the 4- or 5-position has the advantage of preventing inactivation of the compound represented by the above formula (1) by metabolism and maintaining drug efficacy.
  • non-toxic salts formed cation in such salts N a +, K Al force Li metal ions such as +; Mg 2 +, C a 2 alkaline earth such as + metal ions; A 1 3 +, Other non-toxic equivalent metal ions such as Zn2 + ; ammonia; triethylamine, ethylenediamine, propanediamine, pyrrolidine, piperidine, piperazine, pyridine, lysine, choline, ethanolamine, N, N — Organic bases such as dimethylethanolamine, 4-hydroxypiperidine, darcosamine, N-methylglucamine.
  • N a +, C a 2 +, as well as lysine, choline, N, N- dimethylcarbamoyl ethanolamine ⁇ Min be an organic base such as N- methyl dull fluorescamine preferred.
  • the anthranilic acid derivative of the formula (1) or a non-toxic salt thereof may form a pharmaceutically acceptable solvate thereof.
  • Solvents that form such solvates include water, methanol, ethanol, (n- and iso-) propyl alcohol, (n- and tert-) butanol, acetonitrile, acetone, methylethyl. It can be selected from ketone, black form, ethyl acetate, getyl ether, tert-butyl methyl ether, benzene, toluene, DMF, and DMS II.
  • the therapeutic agent for cancer of the present invention contains the above-described anthranilic acid derivative, a pharmaceutically acceptable salt thereof, or a solvate thereof as an active ingredient, and if necessary, is pharmaceutically acceptable. May be added.
  • anthranyl derivative represented by the formula (1) Preferred specific examples of the anthranyl derivative represented by the formula (1) are shown in the following table.
  • these compounds have an asymmetric carbon in the structural formula (for example, compound number 44), all the optical isomers are included, and when the compound has a carbon-carbon double bond,
  • Te t represents a tetrazol-5-yl group.
  • the anthranilic acid derivative which is an active ingredient of the therapeutic agent for cancer of the present invention, has strong cytotoxic activity, as shown in Examples below. Specifically, LC 5.
  • the GI 50 is 5 or less, but preferred is 0.05 nM or more and 1 M or less, more preferably 0.05 nM or more and 500 nM or less.
  • An anthranilic acid derivative having such excellent cytotoxic activity can be used as an active ingredient of a therapeutic agent that can be clinically applied to cancer.
  • the anthranilic acid derivative represented by the above formula (1) or a pharmaceutically acceptable salt thereof can be prepared by those skilled in the art with reference to International Publication WO955Z32943 and International Publication WO9719910. Can be manufactured.
  • RR 2 , X, A, Y, ⁇ , G, and ⁇ are the same as defined above.
  • R 1 Q and R 11 are as defined above.
  • the compounds represented by the formulas [II] and [III], which are starting materials, can be obtained by a known method. Condensation methods are broadly classified into a method using an acid halide and an activation method not using an acid halide, and both methods are basically known.
  • compound [II] or [III] can be converted to a compound such as oxalyl chloride or thionyl chloride with or without an additive such as DMF.
  • the compound [I] is obtained by reacting with a compound [IV] in the presence or absence of a base to produce an acid halide of [II] or [III] by the action of a genating agent be able to.
  • the compound [II] or the compound [II] or a variety of activators such as mixed acid anhydrides, carbodiimides, imidazole agents, halophosphate esters, and cyanophosphate esters are used.
  • activators such as mixed acid anhydrides, carbodiimides, imidazole agents, halophosphate esters, and cyanophosphate esters.
  • compound [I] represents a Y gar COOR 7, and when R 7 represents a lower alkyl group; and G represents a -COOR 3, and R 3 represents a lower alkyl group
  • hydrolysis can be carried out under acidic or basic conditions to convert to a compound in which R 7 or R 3 is a hydrogen atom.
  • the compound [I] thus obtained (where Y represents one COOR 7 and R 7 represents a hydrogen atom; G represents —COOR 3 and R 3 represents a hydrogen atom Or G represents a tetrazole-5-yl group) can be converted to a pharmaceutically acceptable salt as described above, if necessary.
  • an anthranilic acid derivative represented by the above formula (1) or a pharmaceutically acceptable salt thereof, which is an active ingredient of the cancer therapeutic agent of the present invention can be obtained.
  • the therapeutic agent for cancer of the present invention can be administered orally, or parenterally, such as intravenously, subcutaneously, intramuscularly, transdermally, rectally, and instilled, or by inhalation.
  • Examples of the dosage form for oral administration include tablets, pills, granules, powders, solutions, suspensions, syrups, capsules and the like.
  • excipients such as lactose, starch, microcrystalline cellulose; binders such as carboxymethylcellulose, methylcellulose, polyvinylpyrrolidone; sodium alginate, sodium bicarbonate, lauryl It can be molded by a usual method using a disintegrating agent such as sodium sulfate.
  • pills, granules, and powders can be formed by an ordinary method using the above-mentioned excipients and the like.
  • Solutions, suspensions, and syrups include, for example, glycerin esters such as triforce prilin and triacetin; alcohols such as ethanol; water; vegetable oils such as corn oil, cottonseed oil, coconut oil, almond oil, peanut oil, olive oil, and the like. And can be molded by an ordinary method.
  • Capsules are made by filling granules, powders, liquids, or the like, into capsules such as gelatin.
  • Intravenous, subcutaneous and intramuscular dosage forms include injections in the form of sterile aqueous or non-aqueous solutions.
  • aqueous solution for example, physiological saline is used.
  • non-aqueous solution include propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate.
  • isotonic agents preservatives, wetting agents, emulsifiers, dispersants, stabilizers, etc., as necessary. It can be sterilized by appropriately performing such treatments.
  • a sterile solid preparation can be produced and dissolved in sterile water or a sterile solvent for injection immediately before use.
  • Examples of dosage forms for transdermal administration include ointments and creams.
  • Ointments are oils and fats such as castor oil and olive oil; vaseline and the like; creams are fatty oils; diethylene glycol; It is molded by an ordinary method using an emulsifier such as sorbitan monofatty acid ester.
  • suppositories such as gelatin soft capsules are used.
  • Examples of the ophthalmic formulation include aqueous and non-aqueous ophthalmic solutions.
  • Aqueous eye drops use sterile purified water, physiological saline, or an appropriate aqueous solvent as a solvent.
  • Aqueous eye drops using only sterile purified water as a solvent; carboxymethyl cellulose, methyl cellulose, hydroxypropyl cellulose, polyvinylpyrrolidone Viscous ophthalmic solution containing a mucilage such as a surfactant; aqueous suspension ophthalmic solution containing a suspending agent such as a surfactant and a polymer thickener; and a solubilizing agent such as a nonionic surfactant.
  • solubilized eye drops There are solubilized eye drops and the like.
  • Non-aqueous ophthalmic solution is a non-aqueous ophthalmic solution using vegetable oil, liquid paraffin, mineral oil, propylene glycol, etc .; a non-aqueous ophthalmic solution using a thixotropic colloid such as aluminum monostearate.
  • turbid non-aqueous suspension ophthalmic solutions may contain isotonic agents, preservatives, buffers, emulsifiers, stabilizers and the like, if necessary.
  • sterilization can be performed by appropriately performing treatment such as filtration through a bacteria retaining filter, blending of a bactericide, heating, and irradiation.
  • a sterile solid preparation can be produced and dissolved or suspended in an appropriate sterile solution immediately before use.
  • solutions or suspensions of the active ingredients with conventional pharmaceutical excipients are used, for example as aerosol sprays for inhalation.
  • the active ingredient in dry powder form can also be administered by an inhaler or other device that allows direct contact with the lungs.
  • the dosage of the active ingredient of the cancer therapeutic agent of the present invention varies depending on the type of disease, administration route, patient condition, age, gender, body weight, etc., but is usually about 110,000 mgZ per adult person. Yes, it is preferable to formulate such a condition.
  • the active ingredient of the cancer therapeutic agent of the present invention suppresses the proliferation of L929 cells having a strong proliferation at a low concentration. It is also a very useful compound as a carcinostatic because it can inhibit the proliferation of various human cultured cells at the same low concentration.
  • Example 1 the compounds used in the present invention were produced according to the method of Example 1 or Example 2, using the corresponding starting materials.
  • the following table shows the 1 H-NMR spectrum data and reaction yield of the produced compounds.
  • the compound numbers in the table correspond to the compound numbers shown in the table.
  • those ⁇ "is attached to the place of the spectral data is the measurement data of in DMSO- d 6. All others are data measured in CDC 1 3 ⁇ Example Compound Ifl- NMR data (CDC1 3) ⁇ (ppm) Yield
  • this solution was added dropwise to a solution of 59 mg (0.54 mmol) of o-aminophenol and 3 mL of dry pyridine (6 mL) in dry methylene chloride (6 mL) under ice-cooling. Stirred for days. Water was added to the reaction solution, and extracted twice with methylene chloride. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate, and the solvent was distilled off.
  • Example 7 Using 50 mg (0.13 mmo 1) of 2- (4- (2-naphthylthio) benzoic acid amide) benzonitrile obtained in 4 as a starting material, the title compound was obtained in the same manner as in Example 75. 3 mg (77% yield) was obtained.
  • Example 7 2- (3-amino-4- (2-naphthyloxy) benzoic acid amide) obtained in 7) Methyl benzoate (20 Omg (0.48 mmo 1)) was used as a starting material. In the same manner as in the above, 5 lmg (yield 26%) of the title compound was obtained.
  • Example 7 11- (4- (2-naphthyloxy) benzoic acid amide) —2- (tetrazol-5-yl) benzene obtained in 5 to 7-32 mg (1.80 mmo 1) of ethanol in 8 OmL of ethanol Then, 897 mL (1.80 mmol) of a 2 M aqueous sodium hydroxide solution was added to this solution, and the mixture was stirred at room temperature for 2.5 hours. The reaction solution was concentrated, and the remaining transparent film was dissolved in 3 OmL of distilled water. This solution was filtered through a filter (0.45 ⁇ m), and the filtrate was lyophilized to give 767 mg (99% yield) of the title compound as a colorless powder.
  • Example 88 4- (4-Benzyloxyphenoxy) phenylacetamide benzoic acid methyl ester (278 mg, 0.59 mmo 1) obtained in 8 was dissolved in THF (5 mL). To this solution, methanol (5 mL) and a 4M aqueous solution of lithium hydroxide (2 mL) were added, and the mixture was stirred at room temperature for 2 hours. After the completion of the reaction, the obtained reaction solution was neutralized with hydrochloric acid, and concentrated until the liquid amount became half. The crystals formed in the concentrated solution were collected by filtration and dried. Further, the crystals were recrystallized from acetonitrile to obtain 13 Omg (0.29 mmo 1) of the target compound. Yield 49%.
  • Example 8 4.20 g (9. Ommo 1) of ciphenoxy) phenylacetamide) benzoic acid methyl ester were dissolved in ethyl acetate (17 mL). To this solution was added 1-0% palladium on carbon (800 mg) to prepare a reaction mixture. The nitrogen gas was replaced with hydrogen gas, and the reaction mixture was stirred at room temperature for 32 hours. The resulting reaction solution was filtered over celite and concentrated. The obtained concentrate was recrystallized from ethyl acetate to obtain 2.26 g (6. Ommo 1) of the target compound. Yield 66%.
  • Example 98 In the same manner as in Example 98, the compounds shown in the following table were synthesized. The yield of each compound was calculated based on the molar amount of the corresponding raw material methyl ester compound.
  • the cell culture supernatant was removed and washed twice with 200 iL of PBS to remove excess neutral red. Thereafter, 100% tiL of 50% ethanol 1% aqueous acetic acid was added to extract the dye incorporated into the cells, and the amount of the dye was determined by measuring the absorbance at 490 nm. The cytotoxicity was determined for each test compound concentration, taking the case where no drug was added as 100%. For each test compound, by plotting the cytotoxicity of a compound concentration and each concentration was calculated the concentration of test compounds exhibiting 50% cytotoxicity (LD 50 value). In addition, these measurements were performed on two sets of the same conditions, and calculated from the average value. The results are shown in the following table.
  • the therapeutic agent for cancer of the present invention has a cytotoxic effect on highly proliferative cell types, and also has a strong growth inhibitory effect or cytotoxic effect on human cancer cells. Therefore, the therapeutic agent of the present invention can be used as a therapeutic agent for cancer.

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Abstract

L'invention concerne un médicament anticancéreux contenant en tant qu'ingrédient actif un composé représenté par la formule (I). Dans cette formule, X est un groupe représenté par l'une des formules (II) et (III). [R1 et R2 représentent chacun hydrogène, hydroxy, trihalométhyle, alcoxy ou alkylthio C¿1-12?, aralkyloxy C7-11 (substitué) ou alcényloxy C3-10 (substitué) ; R?4 et R5¿ représentent hydrogène, halogéno, alkyle C¿1-4?, ou alcoky C1-4 ; A représente -O-, -S-, -S(=O)-, -S(=O)2-, -CH2-, -OCH2-, -SCH2-, -C(=O)- ou CH(OR?6¿)- ; Y représente hydrogène, halogéno, nitro, nitrile, amino, -COOR7, -NHCOR8 ou NHSO¿2R?9 ; E représente C(=O)-, -CR10R11C(=O)-, -CH¿2?CH2C(=O)- ou CH=CHC(=O)- ; G représente hydrogène, hydroxy, -SO2NH2, -COOR?3¿, -CN ou tétrazol-5-yl ; et Z représente hydrogène, halogéno, nitro ou méthyle.]
PCT/JP2001/001090 2000-02-15 2001-02-15 Medicament anticancereux comprenant un derive d'acide anthranilique en tant qu'ingredient actif WO2001060354A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
AU2001234089A AU2001234089B2 (en) 2000-02-15 2001-02-15 Cancer remedy comprising anthranilic acid derivative as active ingredient
EP01906131A EP1256341A4 (fr) 2000-02-15 2001-02-15 Medicament anticancereux comprenant un derive d'acide anthranilique en tant qu'ingredient actif
CA002400264A CA2400264A1 (fr) 2000-02-15 2001-02-15 Medicament anticancereux comprenant un derive d'acide anthranilique en tant qu'ingredient actif
AU3408901A AU3408901A (en) 2000-02-15 2001-02-15 Cancer remedy comprising anthranilic acid derivative as active ingredient
US10/203,288 US20030220402A1 (en) 2000-02-15 2001-02-15 Cancer remedy comprising anthranilic acid derivatives as active ingredients

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JP2000036386 2000-02-15
JP2000-36386 2000-02-15

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1429765A2 (fr) * 2001-09-14 2004-06-23 Methylgene, Inc. Inhibiteurs de l'histone-deacetylase
US6897220B2 (en) 2001-09-14 2005-05-24 Methylgene, Inc. Inhibitors of histone deacetylase
JP2007530459A (ja) * 2004-03-26 2007-11-01 メシルジーン、インコーポレイテッド ヒストンデアセチラーゼの阻害剤
JP2008546661A (ja) * 2005-06-14 2008-12-25 エフ．ホフマン−ラ ロシュ アーゲー アントラニル酸誘導体
JP2009511499A (ja) * 2005-10-06 2009-03-19 エグゼリクシス， インコーポレイテッド Ｐｉｍ−１および／またはｐｉｍ−３のピリドピリミジノンインヒビター
US7868204B2 (en) 2001-09-14 2011-01-11 Methylgene Inc. Inhibitors of histone deacetylase
US7868205B2 (en) 2003-09-24 2011-01-11 Methylgene Inc. Inhibitors of histone deacetylase
US8088805B2 (en) 2004-03-26 2012-01-03 Methylgene Inc. Inhibitors of histone deacetylase
US8598168B2 (en) 2006-04-07 2013-12-03 Methylgene Inc. Inhibitors of histone deacetylase

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0319124D0 (en) * 2003-08-14 2003-09-17 Smithkline Beecham Corp Chemical compounds
KR100557093B1 (ko) * 2003-10-07 2006-03-03 한미약품 주식회사 다약제 내성 저해 활성을 갖는 테트라졸 유도체 및 그의제조방법
KR100927563B1 (ko) 2004-08-06 2009-11-23 오쓰까 세이야꾸 가부시키가이샤 방향족 화합물
DK1957073T3 (da) 2005-12-05 2014-05-12 Otsuka Pharma Co Ltd Lægemiddel
UA95978C2 (ru) 2006-10-02 2011-09-26 Оцука Фармас'Ютікел Ко., Лтд. Ингибитор активации stat3/5
GB0725214D0 (en) * 2007-12-24 2008-02-06 Karobio Ab Pharmaceutical compounds
EP3044216B1 (fr) * 2013-08-20 2022-02-23 University of Washington through its Center for Commercialization Nouveaux inhibiteurs spécifiques de l'hydroxylase d'acide rétinoïque cytochrome p450 26
BR112021018303A2 (pt) 2019-03-15 2021-11-23 Massachusetts Gen Hospital Novos inibidores de pequenas moléculas de fatores de transcrição tead

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995032943A1 (fr) * 1994-05-31 1995-12-07 Teijin Limited Derive de naphthalene
WO1997019910A1 (fr) * 1995-11-27 1997-06-05 Teijin Limited Derives du benzene
WO2000005198A1 (fr) * 1998-07-24 2000-02-03 Teijin Limited Derives d'acide anthranilique

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2934543A1 (de) * 1979-08-27 1981-04-02 Basf Ag, 6700 Ludwigshafen Substituierte n-benzoylanthranilsaeurederivate und deren anydroverbindungen, verfahren zu ihrer herstellung und ihre verwendung als herbizide
US5705521A (en) * 1990-02-12 1998-01-06 The Center For Innovative Technology Use of allosteric hemoglobin modifiers in combination with radiation therapy to treat carcinogenic tumors
GB9022785D0 (en) * 1990-10-19 1990-12-05 Merck Sharp & Dohme Therapeutic agents
JPH05301838A (ja) * 1991-10-15 1993-11-16 Mitsubishi Kasei Corp スチレン誘導体

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995032943A1 (fr) * 1994-05-31 1995-12-07 Teijin Limited Derive de naphthalene
WO1997019910A1 (fr) * 1995-11-27 1997-06-05 Teijin Limited Derives du benzene
WO2000005198A1 (fr) * 1998-07-24 2000-02-03 Teijin Limited Derives d'acide anthranilique

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1256341A4 *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1429765A2 (fr) * 2001-09-14 2004-06-23 Methylgene, Inc. Inhibiteurs de l'histone-deacetylase
US6897220B2 (en) 2001-09-14 2005-05-24 Methylgene, Inc. Inhibitors of histone deacetylase
US7595343B2 (en) 2001-09-14 2009-09-29 Methylgene, Inc. Inhibitors of histone deacetylase
US7838520B2 (en) 2001-09-14 2010-11-23 Methylgene, Inc. Inhibitors of histone deacetylase
US7868204B2 (en) 2001-09-14 2011-01-11 Methylgene Inc. Inhibitors of histone deacetylase
US7868205B2 (en) 2003-09-24 2011-01-11 Methylgene Inc. Inhibitors of histone deacetylase
JP2007530459A (ja) * 2004-03-26 2007-11-01 メシルジーン、インコーポレイテッド ヒストンデアセチラーゼの阻害剤
US8088805B2 (en) 2004-03-26 2012-01-03 Methylgene Inc. Inhibitors of histone deacetylase
JP2008546661A (ja) * 2005-06-14 2008-12-25 エフ．ホフマン−ラ ロシュ アーゲー アントラニル酸誘導体
US7989657B2 (en) 2005-06-14 2011-08-02 Hoffmann-La Roche Inc. Anthranilic acid derivatives
JP2009511499A (ja) * 2005-10-06 2009-03-19 エグゼリクシス， インコーポレイテッド Ｐｉｍ−１および／またはｐｉｍ−３のピリドピリミジノンインヒビター
US8598168B2 (en) 2006-04-07 2013-12-03 Methylgene Inc. Inhibitors of histone deacetylase

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AU3408901A (en) 2001-08-27
AU2001234089B2 (en) 2005-08-11
EP1256341A4 (fr) 2004-12-08
CA2400264A1 (fr) 2001-08-23
US20030220402A1 (en) 2003-11-27
US20050027008A1 (en) 2005-02-03
EP1256341A1 (fr) 2002-11-13

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